SonoSite C1.9 PLUS, Service Manual

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Chapter 3: System Overview 19
3.5.6.6 Transducers Shipping/Storage
• -31–149°F (-35–65°C), 15–95% R.H
3.5.7 Electrical
• System optional: 100-120/220-240 V ac, 50/60 Hz input, 16.0 V dc output
power adapter
• SiteCharge dual battery charger input voltage: 16.0 V dc, 2.8 A
• SiteCharge dual battery charger output voltage: 12.6 V dc, 3.0 A (2x)
• AC power adapter input: 100-120/220-240 V ac, 50/60 Hz, 1.0-0.50 A
• AC power adapter output: + 16.0 V dc, 2.8 A
3.6 Battery
• 6-cell, 11.1 V dc, 3.0 amp-hours,
rechargeable,
lithium-ion battery pack
• Run time: 1.5 to 4 hours, depending upon operating conditions
3.7 Safety Requirements
3.7.1 Meets Electromechanical Safety Standards
EN 60601-1:1997, European Norm, Medical Electrical Equipment–Part 1. General
Requirements for Safety.
EN 60601-1-1:1993, European Norm, Medical Electrical Equipment–Part 1.
General Requirements for Safety–Section 1-1. Collateral Standard. Safety
Requirements for Medical Electrical Systems.
EN 60601-1-2:1998, European Norm, Medical Electrical Equipment. General
Requirements for Safety-Collateral Standard. Electromagnetic Compatibility.
Requirements and Tests.
EN 60601-2-25: 1996, European Norm, Medical Electrical Equipment–Part 2.
Particular Requirements for Safety–Section 25. Specification for
Electrocardiographs.
C22.2, No. 601.1:1998, Canadian Standards Association, Medical Electrical
Equipment–Part 1. General Requirements for Safety.
CEI/IEC 61157:1992, International Electrotechnical Commission, Requirements for
the Declaration of the Acoustic Output of Medical Diagnostic Ultrasonic
Equipment.
UL 2601-1:1999, Underwriters Laboratories, Medical Electrical Equipment-Part 1:
General Requirements for Safety.